NDC 82018-0008 Biest 2.5 Estrogen Cream (lavender Scented)

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
82018-0008
Proprietary Name:
Biest 2.5 Estrogen Cream (lavender Scented)
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Shyne Brands
Labeler Code:
82018
Start Marketing Date: [9]
06-15-2021
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 82018-0008-2

Package Description: 85 g in 1 BOTTLE, PUMP

Product Details

What is NDC 82018-0008?

The NDC code 82018-0008 is assigned by the FDA to the product Biest 2.5 Estrogen Cream (lavender Scented) which is product labeled by Shyne Brands. The product's dosage form is . The product is distributed in a single package with assigned NDC code 82018-0008-2 85 g in 1 bottle, pump . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Biest 2.5 Estrogen Cream (lavender Scented)?

Uses: This is a topical cream that contains bio-identical estriol and estradiol derived from wild yam and formulated in an 80:20 ratio. When applied to the skin it can help balance your hormones and provide temporary relief from menopausal symptoms such as hot flashes.DIRECTIONS: Apply once or twice a day. Massage into inner arms, thighs, chest or apply to inner forearm and rub arms together or use as directed by your Physician.

Which are Biest 2.5 Estrogen Cream (lavender Scented) UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Biest 2.5 Estrogen Cream (lavender Scented) Inactive Ingredients UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

* Please review the disclaimer below.

Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".